Evidence map›Paper›PMID 17090318›Full record

ArticleBMC bioinformatics2006

Assessing protein similarity with Gene Ontology and its use in subnuclear localization prediction.

Zhengdeng Lei, Yang Dai

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Article in BMC bioinformatics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

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29citing papers in PubMed
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3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

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  6. A weighted multipath measurement based on gene ontology for estimating gene products similarity.Journal of computational biology : a journal of computational molecular cell biology · 2014
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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Zhengdeng LeiDepartment of Bioengineering (MC063), University of Illinois at Chicago, 851 South Morgan Street, Chicago, IL 60607, USA. zlei2@uic.edu <zlei2@uic.edu>
Yang Dai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe accomplishment of the various genome sequencing projects resulted in accumulation of massive amount of gene sequence information. This calls for a large-scale computational method for predicting protein localization from sequence. The protein localization can provide valuable information about its molecular function, as well as the biological pathway in which it participates. The prediction of localization of a protein at subnuclear level is a challenging task. In our previous work we proposed an SVM-based system using protein sequence information for this prediction task. In this work, we assess protein similarity with Gene Ontology (GO) and then improve the performance of the system by adding a module of nearest neighbor classifier using a similarity measure derived from the GO annotation terms for protein sequences.

resultsThe performance of the new system proposed here was compared with our previous system using a set of proteins resided within 6 localizations collected from the Nuclear Protein Database (NPD). The overall MCC (accuracy) is elevated from 0.284 (50.0%) to 0.519 (66.5%) for single-localization proteins in leave-one-out cross-validation; and from 0.420 (65.2%) to 0.541 (65.2%) for an independent set of multi-localization proteins. The new system is available at http://array.bioengr.uic.edu/subnuclear.htm.

conclusionThe prediction of protein subnuclear localizations can be largely influenced by various definitions of similarity for a pair of proteins based on different similarity measures of GO terms. Using the sum of similarity scores over the matched GO term pairs for two proteins as the similarity definition produced the best predictive outcome. Substantial improvement in predicting protein subnuclear localizations has been achieved by combining Gene Ontology with sequence information.

Indexed as

AlgorithmsCell NucleusComputational BiologyComputer SimulationDatabases, ProteinModels, StatisticalPattern Recognition, AutomatedProteinsProteomicsSequence AlignmentSoftwareProteins

Identifiers

PMID17090318
PMCPMC1660555

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.